Candidate genes and functional noncoding variants identified in a canine model of obsessive-compulsive disorder

by Tang, Ruqi, Noh, Hyun Ji, Wang, Dongqing, Sigurdsson, Snaevar, Swofford, Ross, Perloski, Michele, Duxbury, Margaret, Patterson, Edward E., Albright, Julie, Castelhano, Marta, Auton, Adam, Boyko, Adam R., Feng, Guoping, Lindblad-Toh, Kerstin, Karlsson, Elinor K.
Published 2014

Canine Hereditary Ataxia in Old English Sheepdogs and Gordon Setters Is Associated with a Defect in the Autophagy Gene Encoding RAB24

by Agler, Caryline, Nielsen, Dahlia M., Urkasemsin, Ganokon, Singleton, Andrew, Tonomura, Noriko, Sigurdsson, Snaevar, Tang, Ruqi, Linder, Keith, Arepalli, Sampath, Hernandez, Dena, Lindblad-Toh, Kerstin, van de Leemput, Joyce, Motsinger-Reif, Alison, O'Brien, Dennis P., Bell, Jerold, Harris, Tonya, Steinberg, Steven, Olby, Natasha J.
Published 2014

Identification of Genomic Regions Associated with Phenotypic Variation between Dog Breeds using Selection Mapping

by Vaysse, Amaury, Ratnakumar, Abhirami, Derrien, Thomas, Axelsson, Erik, Pielberg, Gerli Rosengren, Fall, Tove, Seppälä, Eija H., Hansen, Mark S. T., Lawley, Cindy T., Bannasch, Danika L., Vilà, Carles, Lohi, Hannes, Galibert, Francis, Fredholm, Merete, Häggström, Jens, Hedhammar, Åke, André, Catherine, Hitte, Christophe, Webster, Matthew T., Sigurdsson, Snaevar, Karlsson, Elinor K, Lindblad-Toh, Kerstin
Published 2012

Genome-wide analyses implicate 33 loci in heritable dog osteosarcoma, including regulatory variants near CDKN2A/B

by Karlsson, Elinor K, Sigurdsson, Snaevar, Ivansson, Emma, Thomas, Rachael, Elvers, Ingegerd, Wright, Jason, Howald, Cedric, Tonomura, Noriko, Perloski, Michele, Swofford, Ross, Biagi, Tara, Fryc, Sarah, Anderson, Nathan, Courtay-Cahen, Celine, Youell, Lisa, Ricketts, Sally L., Mandlebaum, Sarah, Rivera, Patricio, von Euler, Henrik, Kisseberth, William C., London, Cheryl A., Couto, Guillermo, Starkey, Mike P. Comstock, Kenine, Starkey, Mike P., Modiano, Jaime F., Breen, Matthew, Lindblad-Toh, Kerstin, Lander, Eric Steven
Published 2014

Mutations causing medullary cystic kidney disease type 1 lie in a large VNTR in MUC1 missed by massively parallel sequencing

by Kirby, Andrew, Gnirke, Andreas, Jaffe, David B., Baresova, Veronika, Pochet, Nathalie, Blumenstiel, Brendan, Ye, Chun, Aird, Daniel, Stevens, Christine, Robinson, James T., Cabili, Moran N., Gat-Viks, Irit, Kelliher, Edward, Daza, Riza, DeFelice, Matthew, Hulkova, Helena, Sovova, Jana, Vylet'al, Petr, Antignac, Corinne, Guttman, Mitchell, Handsaker, Robert E., Perrin, Danielle, Steelman, Scott, Sigurdsson, Snaevar, Scheinman, Steven J., Sougnez, Carrie, Cibulskis, Kristian, Parkin, Melissa, Green, Todd, Rossin, Elizabeth, Zody, Michael C., Xavier, Ramnik J., Pollak, Martin R., Alper, Seth L., Lindblad-Toh, Kerstin, Gabriel, Stacey B., Hart, P. Suzanne, Regev, Aviv, Nusbaum, Chad, Kmoch, Stanislav, Bleyer, Anthony J., Daly, Mark J., Lander, Eric Steven
Published 2013